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FDA 510(k)

NV CORMED SOLAS SPINAL SYSTEM

K-Number: K051959 · 2005-10-12

ApplicantNv Cormed
Decision Date2005-10-12
Product CodeMNH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NV CORMED SOLAS SPINAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Nv Cormed. It received FDA 510(k) clearance on 2005-10-12 under 510(k) number K051959. The device is classified under product code MNH. It was reviewed by the OR advisory panel. Product code MNH falls under the category of ENT, which includes ear, nose, and throat diagnostic and surgical devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NV CORMED SOLAS SPINAL SYSTEM?

NV CORMED SOLAS SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 2005-10-12. The listed applicant is Nv Cormed. The 510(k) number is K051959.

When did NV CORMED SOLAS SPINAL SYSTEM receive FDA 510(k) clearance?

NV CORMED SOLAS SPINAL SYSTEM received FDA 510(k) clearance on 2005-10-12, under 510(k) number K051959.

Who is the listed applicant for NV CORMED SOLAS SPINAL SYSTEM?

The FDA 510(k) record lists Nv Cormed as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NV CORMED SOLAS SPINAL SYSTEM?

The FDA product code for NV CORMED SOLAS SPINAL SYSTEM is MNH. This falls under the ENT category.

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Related Devices (Code: MNH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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